分析化学
分析化學
분석화학
CHINESE JOURNAL OF ANALYTICAL CHEMISTRY
2014年
12期
1842-1845
,共4页
刘丹华%唐红芳%刘绿叶%金燕%朱海豹%阮征%钱亚玲
劉丹華%唐紅芳%劉綠葉%金燕%硃海豹%阮徵%錢亞玲
류단화%당홍방%류록협%금연%주해표%원정%전아령
N-乙酰-S-(N-甲基甲氨酰)半胱氨酸%在线固相萃取%高效液相色谱%人体尿液
N-乙酰-S-(N-甲基甲氨酰)半胱氨痠%在線固相萃取%高效液相色譜%人體尿液
N-을선-S-(N-갑기갑안선)반광안산%재선고상췌취%고효액상색보%인체뇨액
N-Acetyl-S-( N-methylcarbamoyl ) cysteine%Online solid phase extraction%High performance liquid chromatography%Human urine
建立了在线固相萃取-高效液相色谱法测定人体尿液中的N-乙酰-S-( N-甲基甲氨酰)半胱氨酸( AM-CC)的分析方法。左泵以AminoPac PA柱作为在线固相萃取柱、5 mmol/L KH2 PO4溶液为流动相,将AMCC与样品基质分离;然后通过控制阀切换时间仅将含AMCC的部分样品溶液在线洗脱至Acclaim PAⅡ C18分析柱上,右泵以0.1% H3 PO4溶液(含5%乙腈)和乙腈为流动相对AMCC进行梯度洗脱分离和分析测定。结果表明,AMCC在1.0~100 mg/L范围内线性关系良好,相关系数r>0.999;上样量为10μL时,方法定量限为0.2 mg/L;回收率在85.9%~82.9%之间;相对标准偏差(n=6)分别为0.2%(保留时间)和4.0%(峰面积)。与传统的离线固相萃取-高效液相色谱法相比,本方法更为简便环保、高效稳定。用本方法测定了7份人体尿液,结果满意。
建立瞭在線固相萃取-高效液相色譜法測定人體尿液中的N-乙酰-S-( N-甲基甲氨酰)半胱氨痠( AM-CC)的分析方法。左泵以AminoPac PA柱作為在線固相萃取柱、5 mmol/L KH2 PO4溶液為流動相,將AMCC與樣品基質分離;然後通過控製閥切換時間僅將含AMCC的部分樣品溶液在線洗脫至Acclaim PAⅡ C18分析柱上,右泵以0.1% H3 PO4溶液(含5%乙腈)和乙腈為流動相對AMCC進行梯度洗脫分離和分析測定。結果錶明,AMCC在1.0~100 mg/L範圍內線性關繫良好,相關繫數r>0.999;上樣量為10μL時,方法定量限為0.2 mg/L;迴收率在85.9%~82.9%之間;相對標準偏差(n=6)分彆為0.2%(保留時間)和4.0%(峰麵積)。與傳統的離線固相萃取-高效液相色譜法相比,本方法更為簡便環保、高效穩定。用本方法測定瞭7份人體尿液,結果滿意。
건립료재선고상췌취-고효액상색보법측정인체뇨액중적N-을선-S-( N-갑기갑안선)반광안산( AM-CC)적분석방법。좌빙이AminoPac PA주작위재선고상췌취주、5 mmol/L KH2 PO4용액위류동상,장AMCC여양품기질분리;연후통과공제벌절환시간부장함AMCC적부분양품용액재선세탈지Acclaim PAⅡ C18분석주상,우빙이0.1% H3 PO4용액(함5%을정)화을정위류동상대AMCC진행제도세탈분리화분석측정。결과표명,AMCC재1.0~100 mg/L범위내선성관계량호,상관계수r>0.999;상양량위10μL시,방법정량한위0.2 mg/L;회수솔재85.9%~82.9%지간;상대표준편차(n=6)분별위0.2%(보류시간)화4.0%(봉면적)。여전통적리선고상췌취-고효액상색보법상비,본방법경위간편배보、고효은정。용본방법측정료7빈인체뇨액,결과만의。
A method was developed for the determination of N-acetyl-S-( N-methylcarbamoyl ) cysteine ( AMCC) in human urine by online solid-phase extraction ( SPE )-high performance liquid chromatography ( HPLC ) . The separation of AMCC from the urine matrix was performed on AmoniPac PA Solid phase Extraction ( SPE ) column with 5 mmol/L KH2 PO4 as the mobile phase by left pump. Then the time was controlled to switch the valve to make only the section of sample containing AMCC transferred into the analytic column-Acclaim PAⅡ C18 . The determination was performed using gradient elution of 0. 1% H3 PO4 (containing 5% acetonitrile) and acetonitrile by right pump. The results showed that AMCC present good linear correlation in the range of 1 . 0-100 mg/L with a correlation coefficient of above 0 . 999 , the quantitation limit of the method was 0. 2 mg/L (with the sample inject volume =10 μL), the recoveries of spiked samples were in the range of 82 . 9%-85 . 9%, and the relative standard deviation ( n=6 ) of retention time and peak area were 0. 2% and 4. 0% respectively. Compared with offline SPE-HPLC, the proposed method was convenient, environmentally friendly, efficient and stable, and feasible for the detection of AMCC in 7 human urine samples.